Is N-Acetyl-Cysteine, 600 MG, CAPSULE, Distributed by: AidaPak Service, LLC, NDC 27434-0002-11. recalled?

Medium RiskFDA Drug

Aidapak Services, LLC: Penicillin Cross Contamination; There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility.; There is a potential for Penicillin cross contamination; Penicillin Cross Contamination; There is potential for beta-lactam cross contamination of non-penicillin drug products repackaged in the same facility.There is a potential for Penicillin cross contamination; Penicillin Cross Contamination: There is potential for beta

Agency Publication Date: October 4, 2011

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 59237

Status: Resolved

Manufacturer: Aidapak Services, LLC

Manufactured In: United States

Units Affected: 221 products (840 Capsules; 198 Tablets; 99 Tablets; 11,107 Tablets; 1000 Tablets; 14,573 Tablets; 449 tablets; 100 tablets; 399 tablets; 668 tablets; 778 tablets; 120 tablets; 120 tablets; 755 tablets; 840 tablets; 220 tablets; 180 tablets; 100 tablets; 200 tablets; 99 tablets; 99 capsules; 400 tablets; 1,398 tablets; 99 tablets; 2,736 Tablets; 1,298 capsules; 6,401 tablets; 90 tablets; 8,849 tablets; 1,901 capsules; 89 capsules; 90 capsules; 4,670 lozenges; 428 lozenges; 7,068 pieces; 299 capsules; 6,823 capsules; 200 capsules; 300 tablets; 200 tablets; 100 tablets; 100 tablets; 400 tablets; 1,080 cups; 100 capsules; 1,499 capsules; 100 capsules; 299 capsules; 498 capsules; 199 tablets; 20 tablets; 399 capsules; 699 capsules; 398 capsules; 1,096 capsules; 99 tablets; 475 cups; 1,440 tablets; 90 tablets; 29 tablets; 30 tablets; 60 tablets; 30 tablets; 357 tablets; 200 capsules; 260 capsules; 185,187 softgels; 23,638 capsules; 2,300 softgels; 150 capsules; 358 capsules; 64,741 capsules; 180 tablets; 21 cups; 2279 tablets; 299 tablets; 198 tablet; 300 tablets; 4525 cups; 2976 tablets; 399 tablets; 99 tablets; 800 tablets; 414 tablets; 99 capsules; 200 Tablets; 398 Tablets; 400 Capsules; 2443 capsules; 3591 Capsules; 1098 Capsules; 100 Capsules; 1898 capsules; 1190 Tablets; 15,867 Tablets; 266 capsules; 1222 tablets; 698 tablets; 2096 tablets; 1022 tablets; 416 tablets; 84 suppositories; 53 suppositories; 156 suppositories; 3100 tablets; 4600 tablet; 995 Capsules; 797 tablets; 18,273 tablets; 599 tablets; 4300 tablets; 1200 tablets; 799 tablets; 300 tablets; 60 tablets; 100 tablets; 300 tablets; 200 tablets; 26,282 cups; 59 cups; 4101 capsules; 3985 capsules; 6582 tablets; 3038 tablets; 400 tablets; 100 tablets; 400 tablets; 200 tablets; 8581 tablets; 4504 tablet; 1254 tablets; 498 capsules; 799 capsules; 29 tablets; 500 chew tablets; 1196 tablets; 102 syringes; 3834 syringes; 600 tablets; 999 capsules; 99 capsules; 200 capsules; 100 capsules; 472 syringes; 31 syringes; 300 tablets; 99 tablets; 100 tablets; 100 tablets; 717 tablets; 270 tablets; 604 tablets; 909 tablets; 358 tablets; 720 tablets; 90 tablets; 688 tablets; 5155 tablets; 499 capsules; 1000 capsules; 99 capsules; 19,003 cups and syringes; 144 cups; 1 tablet; 899 tablets; 92 cups; 1344 capsules; 270 capsules; 27 tablets; 5570 tablets; 100 tablets; 400 tablets; 300 tablets; 11,094 tablets; 200 tablets; 27,347 tablets; 9179 tablets; 9995 tablets; 200 tablets; 540 capsules; 199 tablets; 199 tablets; 1299 tablets; 499 tablets; 997 tablets; 5721 capsules; 298 capsules; 100 capsules; 597 capsules; 7794 tablets; 3388 cups; 92 cups; 1054 cups; 21 cups; 120 capsules; 99 tablets; 120 capsules; 895 tablets; 100 capsules; 700 tablets; 99 tablets; 3188 tablets; 3359 capsules; 1400 capsules; 790 capsules; 906 tablets; 297 tablets; 1193 tablets; 220 syringes; 815 tablets; 115 cups; 2195 tablets; 159 tablets; 120 tablets; 599 tablets; 800 tablets; 99 tablets; 100 tablets; 27,006 tablets; 100 tablets; 99 capsules)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.